A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059720



Internal ID21479981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108023436..108023534hg38UCSC Ensembl
chr1:108566058..108566156hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582422
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059720
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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